Docking Proteins Upregulate IL-1β Expression in Lower Esophageal Sphincter Muscle in Esophageal Achalasia.
Tsutomu KandaKaren SaikiHiroki KurumiAkira YoshidaYuichiro IkebuchiTakuki SakaguchiShigetoshi UrabeHitomi MinamiNaoyuki YamaguchiKazuhiko NakaoHaruhiro InoueHajime IsomotoPublished in: Journal of clinical medicine (2024)
Background/Objectives: Esophageal achalasia is an archetypal esophageal motility disorder characterized by abnormal peristalsis of the esophageal body and impaired lower esophageal sphincter (LES) relaxation. Methods: In this study, the mRNA expression of docking proteins 1 and 2 ( DOK1 and DOK2 , respectively) were analyzed and the mechanisms underlying achalasia onset were investigated. Results: DOK1 and DOK2 mRNA levels significantly increased in the LES of patients with achalasia. Moreover, significant correlations were observed between IL-1β and DOK1 , IL-1β and DOK2 , ATG16L1 and DOK1 , and HSV1-miR-H1-3p and DOK2 expression levels. However, a correlation between ATG16L1 and DOK2 or between HSV-miR-H1-3p and DOK1 expression was not observed. In addition, a positive correlation was observed between patient age and DOK1 expression. Microarray analysis revealed a significant decrease in the expression of hsa-miR-377-3p and miR-376a-3p in the LES muscle of patients with achalasia. Conclusions: These miRNAs possessed sequences targeting DOK. The upregulation of DOK1 and DOK2 expression induces IL-1β expression in the LES of achalasia patients, which may contribute to the development of esophageal motility disorder.
Keyphrases
- poor prognosis
- long non coding rna
- binding protein
- cell proliferation
- skeletal muscle
- molecular dynamics
- signaling pathway
- escherichia coli
- newly diagnosed
- staphylococcus aureus
- pseudomonas aeruginosa
- chronic kidney disease
- high resolution
- small molecule
- protein protein
- prognostic factors
- cystic fibrosis
- single cell
- urinary incontinence
- genetic diversity